NDC 69457-000 Red Serum
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69457-000?
What are the uses for Red Serum?
Which are Red Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- WITCH HAZEL (UNII: 101I4J0U34)
- WITCH HAZEL (UNII: 101I4J0U34) (Active Moiety)
Which are Red Serum Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BETAINE (UNII: 3SCV180C9W)
- PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)
- VACCINIUM ANGUSTIFOLIUM WHOLE (UNII: R3538BZ1BW)
- RUBUS CHAMAEMORUS FRUIT (UNII: 74CW8G72Q6)
- LYCIUM CHINENSE FRUIT (UNII: TG711Q7A1Q)
- RUBUS IDAEUS FRUIT VOLATILE OIL (UNII: 276X2YNL0K)
- EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
- LEPIDIUM SATIVUM LEAF (UNII: 2ML4POY35W)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DIOSCOREA OPPOSITIFOLIA WHOLE (UNII: KZY1A7K8MD)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
- ALMOND OIL (UNII: 66YXD4DKO9)
- PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
- ALLANTOIN (UNII: 344S277G0Z)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- ARGININE (UNII: 94ZLA3W45F)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ADENOSINE (UNII: K72T3FS567)
- JASMINUM OFFICINALE WHOLE (UNII: X3314B4SYD)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".